FDA inspection
ILMO PRODUCTS COMPANY: FDA inspection ending Jun 28, 2012
FDA inspection 788519 · No Action Indicated (NAI) · Jacksonville, IL
Key facts
| Inspection ID | 788519 |
|---|---|
| Firm | ILMO PRODUCTS COMPANY |
| FEI number | 1454831 |
| Address | 7 Eastgate Dr |
| City | Jacksonville |
| State | IL |
| ZIP | 62650 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Jun 28, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data